GrbichC, AbernethyAP, Shelby-JamesT, FazekasB, CurrowDC. Creating a research culture in a palliative care service environment: A qualitative study of the evolution of staff attitudes to research during a large longitudinal controlled trial. J Palliat Care, 2008; 24,2:100–109ISRCTN81117481.
2.
CurrowDC, EagarK, AounS, FildesD, YatesP, KristjansonLJ. Is it feasible and desirable to collect voluntarily quality and outcome data nationally in palliative oncology care?J Clin Oncol, 2008; 26,23:3853–3859.
3.
KamalAH, CurrowDC, RitchieC, BullJ, WheelerJL, AbernethyAP. The value of data collection within a palliative care program. Curr Oncol Rep, 2011; 13,4:308–315.
4.
AbernethyAP, BaschE, BullJ, CleelandCS, CurrowDC, FaircloughD, HansonL, HauserJ, KoD, LloydL, MorrisonS, Otis-GreenS, PantilatS, PortenoyRK, RitchieC, RockerG, WheelerJL, ZafarSY, KutnerJS. A strategy to advance the evidence base in Palliative Medicine: Formation of a Palliative Care Research Cooperative group. J Palliat Med, 2010; 13,12:1407–1413.
5.
SigurdardottirKR, HaugenDF, BauseweinC, HigginsonIJ, HardingR, RoslandJH, KaasaS. Project PRISMA: A pan-European survey of research in end-of-life cancer care. Support Care Cancer, 2012; 20,1:39–48.
6.
HickmanS, CartwrightJ, NelsonC, KnaflK. Compassion and vigilance: Investigators' strategies to manage ethical concerns in palliative and end-of-life research. J Palliat Med, 2012; 15,8:880–889.
